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Unconventional Roles of the NADPH Oxidase: Signaling, Ion Homeostasis, and Cell Death

https://doi.org/10.1126/stke.3792007pe11

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jlb.59.2.229openalex-snapshot

Rapid killing of human neutrophils by the potent activator phorbol 12-myristate 13-acetate (PMA) accompanied by changes different from typical apoptosis or necrosis

inferredcites →https://doi.org/10.1002/jlb.65.2.196openalex-snapshot

Activation of the granule pool of the NADPH oxidase accelerates apoptosis in human neutrophils

inferredcites →https://doi.org/10.1016/j.cell.2005.05.016openalex-snapshot

Redox Redux: Revisiting PTPs and the Control of Cell Signaling

inferredcites →https://doi.org/10.1016/j.cell.2006.05.035openalex-snapshot

NOX2 Controls Phagosomal pH to Regulate Antigen Processing during Crosspresentation by Dendritic Cells

inferredcites →https://doi.org/10.1016/j.coi.2003.12.001openalex-snapshot

NADPH oxidase

inferredcites →https://doi.org/10.1016/j.cub.2005.12.039openalex-snapshot

DNase Expression Allows the Pathogen Group A Streptococcus to Escape Killing in Neutrophil Extracellular Traps

inferredcites →https://doi.org/10.1016/j.cub.2006.01.056openalex-snapshot

An Endonuclease Allows Streptococcus pneumoniae to Escape from Neutrophil Extracellular Traps

inferredcites →https://doi.org/10.1016/j.humimm.2005.11.003openalex-snapshot

Induction of Neutrophil Extracellular DNA Lattices by Placental Microparticles and IL-8 and Their Presence in Preeclampsia

inferredcites →https://doi.org/10.1016/j.yexcr.2006.08.022openalex-snapshot

NADPH oxidase-derived ROS: Key modulators of heme-induced mitochondrial stability in human neutrophils

inferredcites →https://doi.org/10.1038/290406a0openalex-snapshot

The respiratory burst of phagocytic cells is associated with a rise in vacuolar pH

inferredcites →https://doi.org/10.1038/nri1312openalex-snapshot

NOX enzymes and the biology of reactive oxygen

inferredcites →https://doi.org/10.1073/pnas.0607914103openalex-snapshot

SK channels mediate NADPH oxidase-independent reactive oxygen species production and apoptosis in granulocytes

inferredcites →https://doi.org/10.1074/jbc.272.42.26471openalex-snapshot

Regulation of Capacitative Ca2+ Influx in Human Neutrophil Granulocytes

inferredcites →https://doi.org/10.1074/jbc.274.37.26098openalex-snapshot

A Noninvasive Fluorimetric Procedure for Measurement of Membrane Potential

inferredcites →https://doi.org/10.1074/jbc.274.51.36817openalex-snapshot

Resistance to the Cytotoxic Effects of Tumor Necrosis Factor α Can Be Overcome by Inhibition of a FADD/Caspase-dependent Signaling Pathway

inferredcites →https://doi.org/10.1074/jbc.m003280200openalex-snapshot

Sensitization to Death Receptor Cytotoxicity by Inhibition of Fas-associated Death Domain Protein (FADD)/Caspase Signaling

inferredcites →https://doi.org/10.1074/jbc.m210727200openalex-snapshot

Elucidation of Molecular Events Leading to Neutrophil Apoptosis following Phagocytosis

inferredcites →https://doi.org/10.1083/jcb.200606027openalex-snapshot

Novel cell death program leads to neutrophil extracellular traps

inferredcites →https://doi.org/10.1084/jem.20052069openalex-snapshot

Neutrophils from p40phox−/− mice exhibit severe defects in NADPH oxidase regulation and oxidant-dependent bacterial killing

inferredcites →https://doi.org/10.1084/jem.20052085openalex-snapshot

The phosphoinositide-binding protein p40phox activates the NADPH oxidase during FcγIIA receptor–induced phagocytosis

inferredcites →https://doi.org/10.1098/rstb.2005.1768openalex-snapshot

Consequences of the electrogenic function of the phagocytic NADPH oxidase

inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot

Neutrophil Extracellular Traps Kill Bacteria

inferredcites →https://doi.org/10.1152/ajpcell.1986.251.1.c55openalex-snapshot

Cytoplasmic pH regulation in phorbol ester-activated human neutrophils

inferredcites →https://doi.org/10.1152/physrev.00044.2005openalex-snapshot

The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology

inferredcites →https://doi.org/10.1172/jci116587openalex-snapshot

Transient elevations of cytosolic free calcium retard subsequent apoptosis in neutrophils in vitro.

inferredcites →https://doi.org/10.1182/blood-2001-12-0266openalex-snapshot

Broad-spectrum caspase inhibition paradoxically augments cell death in TNF-α–stimulated neutrophils

inferredcites →https://doi.org/10.1182/blood-2002-02-0522openalex-snapshot

Tumor necrosis factor α induces a caspase-independent death pathway in human neutrophils

inferredcites →https://doi.org/10.1182/blood-2004-03-1005openalex-snapshot

Dual role of phagocytic NADPH oxidase in bacterial killing

inferredcites →https://doi.org/10.1182/blood.v100.9.3383openalex-snapshot

Cytosolic pH and the inflammatory microenvironment modulate cell death in human neutrophils after phagocytosis

inferredcites →https://doi.org/10.1182/blood.v89.5.1748openalex-snapshot

Involvement of Reactive Oxygen Intermediates in Spontaneous and CD95(Fas/APO-1)–Mediated Apoptosis of Neutrophils

inferredcites →https://doi.org/10.1182/blood.v92.12.4808openalex-snapshot

Involvement of Caspases in Neutrophil Apoptosis: Regulation by Reactive Oxygen Species

inferredcites →https://doi.org/10.1189/jlb.0506359openalex-snapshot

Cathepsin-cleaved Bid promotes apoptosis in human neutrophils via oxidative stress-induced lysosomal membrane permeabilization

inferredcites →https://doi.org/10.1189/jlb.71.5.775openalex-snapshot

Oxidant-mediated phosphatidylserine exposure and macrophage uptake of activated neutrophils: possible impairment in chronic granulomatous disease

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Biomarkers of peripheral blood neutrophil extracellular traps in the diagnosis and progression of malignant tumors

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Spatiotemporal histological changes observed in mouse subcutaneous tissues during the foreign body reaction to silicone

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Reactive oxygen species‐induced activation of ERK and p38 MAPK mediates PMA‐induced NETs release from human neutrophils

inferred← citeshttps://doi.org/10.1002/jobm.202100133openalex-snapshot

Apoptosis‐like death‐inducing property of tachyplesin I in Escherichia coli

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In Vitro Identification and Isolation of Human Neutrophil Extracellular Traps

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Neutrophils in Acute Bacterial Pneumonia

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What Is the Pathobiology of Inflammation to Cell Death? Apoptosis, Necrosis, Necroptosis, Autophagic Cell Death, Pyroptosis, and NETosis

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Key mechanisms governing resolution of lung inflammation

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Age is the work of art? Impact of neutrophil and organism age on neutrophil extracellular trap formation

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Neutrophils in tissue injury and repair

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The behavior of neutrophil extracellular traps and NADPH oxidative activity in pediatric systemic lupus erythematosus: relation to disease activity and lupus nephritis

inferred← citeshttps://doi.org/10.1007/s10741-024-10421-xopenalex-snapshot

The role of NETosis in heart failure

inferred← citeshttps://doi.org/10.1007/s10989-012-9290-3openalex-snapshot

In Vitro Modulation of E. coli Community Behavior and Human Innate Immune System by Lantibiotic Nisin

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Emerging paradigms in arterial thrombosis

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Neutrophil Extracellular Trapping Role in Cancer, Metastases, and Cancer-Related Thrombosis: a Narrative Review of the Current Evidence Base

inferred← citeshttps://doi.org/10.1007/s11926-020-00936-1openalex-snapshot

NETs in APS: Current Knowledge and Future Perspectives

inferred← citeshttps://doi.org/10.1007/s12011-020-02477-1openalex-snapshot

Effect of Copper, Zinc, and Selenium on the Formation of Bovine Neutrophil Extracellular Traps

inferred← citeshttps://doi.org/10.1007/s12274-021-3685-4openalex-snapshot

Boron doped graphdiyne: A metal-free peroxidase mimetic nanozyme for antibacterial application

inferred← citeshttps://doi.org/10.1007/s13346-022-01243-1openalex-snapshot

Neutrophils and neutrophil extracellular traps in cancer: promising targets for engineered nanomaterials

inferred← citeshttps://doi.org/10.1007/s40279-014-0296-1openalex-snapshot

Neutrophil Extracellular Traps: A Walk on the Wild Side of Exercise Immunology

inferred← citeshttps://doi.org/10.1007/s40520-022-02201-0openalex-snapshot

Aging hampers neutrophil extracellular traps (NETs) efficacy

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ACINUS: a putative integrant of programmed cell death in plants

inferred← citeshttps://doi.org/10.1016/b978-0-12-397169-2.00038-xopenalex-snapshot

Streptococcus pyogenes

inferred← citeshttps://doi.org/10.1016/b978-0-12-800262-9.00001-9openalex-snapshot

Pseudomonas aeruginosa Biofilms

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Neutrophil-Mediated Vascular Host Defense

inferred← citeshttps://doi.org/10.1016/b978-0-12-801899-6.00025-5openalex-snapshot

Circulating Histones and Nucleosomes as Biomarkers in Sepsis and Septic Shock

inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.00002-2openalex-snapshot

Eosinophil cell death

inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.09990-1openalex-snapshot

References

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NETosis: mechanisms and antimicrobial strategies

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Streptococcus pyogenes

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Neutrophil extracellular traps in autoimmunity, renal diseases, and transplantation

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Visualizing and mapping cell death: Biochemical tools, techniques and assays

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Formation and Disordered Degradation of Neutrophil Extracellular Traps in Necrotizing Lesions of Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis

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Neutrophil extracellular traps and their role in the development of chronic inflammation and autoimmunity

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An emerging role of neutrophils and NETosis in chronic inflammation and fibrosis in systemic lupus erythematosus (SLE) and ANCA-associated vasculitides (AAV): Implications for the pathogenesis and treatment

inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165664openalex-snapshot

Mitochondrial permeability transition pore is involved in oxidative burst and NETosis of human neutrophils

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The role and mechanism of extracellular traps in chronic rhinosinusitis

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Neutrophils and NETosis in Alzheimer’s disease: Unraveling pathogenic mechanisms and novel therapeutic targets

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Entosis: The emerging face of non-cell-autonomous type IV programmed death

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NETosis markers: Quest for specific, objective, and quantitative markers

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Phagocyte extracellular traps formation contributes to host defense against Clostridium perfringens infection

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Peptidylarginine deiminases: physiological function, interaction with chemokines and role in pathology

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Effect of propiconazole on neutrophil extracellular traps formation: Assessing the role of autophagy

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Recent advances in chronic granulomatous disease

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Effects of the antioxidants Trolox, Tiron and Tempol on neutrophil extracellular trap formation

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Highlighting the versatility of the citrullination process

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Silver nanoparticles rapidly induce atypical human neutrophil cell death by a process involving inflammatory caspases and reactive oxygen species and induce neutrophil extracellular traps release upon cell adhesion

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Protein Kinase C Isoforms Mediate the Formation of Neutrophil Extracellular Traps

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Rethinking neutrophil extracellular traps

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DNase based therapeutic approaches for the treatment of NETosis related inflammatory diseases

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Expanding the B Cell-Centric View of Systemic Lupus Erythematosus

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Neutrophil extracellular traps: Formation, pathological roles, and nanoparticle-based therapeutic targeting strategies

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Neutrophil extracellular traps in dermatology: Caught in the NET

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Extracellular Trap Formation by Donkey Polymorphonuclear Neutrophils Against Toxoplasma gondii

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Abnormal neutrophil traps and impaired efferocytosis contribute to liver injury and sepsis severity after binge alcohol use

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The Role of Crosstalk between Nets and Keratinocytes in Skin Immunity

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The role of neutrophils and neutrophil extracellular traps in Staphylococcus aureus colonization in healthy and inflamed skin

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Swine spermatozoa trigger aggregated neutrophil extracellular traps leading to adverse effects on sperm function

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Characterization of systemic neutrophil function in patients undergoing colorectal cancer resection

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NETosis in ischemic/reperfusion injuries: An organ-based review

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Eosinophils: Focus on DNA extracellular traps

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HMGB1 in health and disease

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Trampas extracelulares de neutrófilos: un mecanismo de defensa con dos caras

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Extracellular traps are associated with human and mouse neutrophil and macrophage mediated killing of larval Strongyloides stercoralis

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Multi-facets of neutrophil extracellular trap in infectious diseases: Moving beyond immunity

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NETs detection and quantification in paraffin embedded samples using confocal microscopy

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NETosis in ischemic stroke: Mechanisms, implications, and therapeutic prospects

inferred← citeshttps://doi.org/10.1016/j.phrs.2021.105779openalex-snapshot

Neutrophil extracellular traps in inflammatory bowel diseases: Implications in pathogenesis and therapeutic targets

inferred← citeshttps://doi.org/10.1016/j.preghy.2020.03.007openalex-snapshot

Neutrophil extracellular traps: The synergy source in the placentae of HIV infected women with pre-eclampsia

inferred← citeshttps://doi.org/10.1016/j.redox.2019.101255openalex-snapshot

Mitochondria as central hub of the immune system

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The many roles of myeloperoxidase: From inflammation and immunity to biomarkers, drug metabolism and drug discovery

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Investigating neutrophil responses to stimuli: Comparative analysis of reactive species-dependent and independent mechanisms

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The association between white blood cell count and outcomes in patients with idiopathic pulmonary fibrosis

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Human neutrophils in auto-immunity

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Chronic obstructive pulmonary disease: From mechanistic insights to therapeutic strategies

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Tocilizumab improves the proatherothrombotic profile of rheumatoid arthritis patients modulating endothelial dysfunction, NETosis, and inflammation

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Turning the Spotlight on Lipids in Non-Apoptotic Cell Death

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Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality

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Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012

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Initiation and execution mechanisms of necroptosis: an overview

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Neutrophil extracellular trap cell death requires both autophagy and superoxide generation

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Elevated fecal calprotectin levels during necrotizing enterocolitis are associated with activated neutrophils extruding neutrophil extracellular traps

inferred← citeshttps://doi.org/10.1038/ncomms10938openalex-snapshot

Social amoebae trap and kill bacteria by casting DNA nets

inferred← citeshttps://doi.org/10.1038/nrmicro1710openalex-snapshot

Beneficial suicide: why neutrophils die to make NETs

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To NET or not to NET:current opinions and state of the science regarding the formation of neutrophil extracellular traps

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Uncovering the multifaceted roles played by neutrophils in allogeneic hematopoietic stem cell transplantation

inferred← citeshttps://doi.org/10.1038/s41598-017-16778-4openalex-snapshot

Mineral particles stimulate innate immunity through neutrophil extracellular traps containing HMGB1

inferred← citeshttps://doi.org/10.1038/s41598-018-32576-yopenalex-snapshot

Respiratory Syncytial Virus induces the classical ROS-dependent NETosis through PAD-4 and necroptosis pathways activation

inferred← citeshttps://doi.org/10.1038/s41598-019-44379-wopenalex-snapshot

Neutrophil Extracellular Traps protein composition is specific for patients with Lupus nephritis and includes methyl-oxidized αenolase (methionine sulfoxide 93)

inferred← citeshttps://doi.org/10.1038/s41598-019-57173-5openalex-snapshot

Leukocyte-derived extracellular DNA contributes to abnormal pressure elevation in the extracorporeal circulation circuit

inferred← citeshttps://doi.org/10.1038/s41598-021-85561-3openalex-snapshot

S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils

inferred← citeshttps://doi.org/10.1038/srep36362openalex-snapshot

Elevated homocysteine levels in type 2 diabetes induce constitutive neutrophil extracellular traps

inferred← citeshttps://doi.org/10.1038/srep41749openalex-snapshot

Transcriptional firing helps to drive NETosis

inferred← citeshttps://doi.org/10.1039/d6mh00654jopenalex-snapshot

Nanomedicine-mediated programmed necrosis for cancer immunosurveillance

inferred← citeshttps://doi.org/10.1080/00365513.2017.1419371openalex-snapshot

Calprotectin (S100A8/A9) should preferably be measured in EDTA-plasma; results from a longitudinal study of patients with rheumatoid arthritis

inferred← citeshttps://doi.org/10.1080/08830185.2021.1921174openalex-snapshot

Neutrophil extracellular trap-associated molecules: a review on their immunophysiological and inflammatory roles

inferred← citeshttps://doi.org/10.1080/08923973.2022.2088386openalex-snapshot

Rituximab induces a flare-up of activated neutrophil extracellular traps under in vitro conditions

inferred← citeshttps://doi.org/10.1080/08927014.2021.2002987openalex-snapshot

Tracing the origins of extracellular DNA in bacterial biofilms: story of death and predation to community benefit

inferred← citeshttps://doi.org/10.1083/jcb.201203170openalex-snapshot

Neutrophil extracellular traps: Is immunity the second function of chromatin?

inferred← citeshttps://doi.org/10.1089/ars.2009.2558openalex-snapshot

Mechanisms and Function of DUOX in Epithelia of the Lung

inferred← citeshttps://doi.org/10.1093/femspd/ftaa018openalex-snapshot

The origin of extracellular DNA in bacterial biofilm infections in vivo

inferred← citeshttps://doi.org/10.1093/infdis/jix475openalex-snapshot

High Level of Neutrophil Extracellular Traps Correlates With Poor Prognosis of Severe Influenza A Infection

inferred← citeshttps://doi.org/10.1097/md.0000000000002580openalex-snapshot

Clinicopathologic Characteristics and Outcomes of Lupus Nephritis With Antineutrophil Cytoplasmic Antibody

inferred← citeshttps://doi.org/10.1097/md.0000000000033806openalex-snapshot

Mapping current status and emerging trends in NETosis: A bibliometric study

inferred← citeshttps://doi.org/10.1097/ms9.0000000000004785openalex-snapshot

Roles of anesthetics in modulating neutrophil extracellular traps formation: a review of current literature

inferred← citeshttps://doi.org/10.1097/shk.0000000000000221openalex-snapshot

Neutrophil Extracellular Traps in Sepsis

inferred← citeshttps://doi.org/10.1101/2024.07.09.24310187openalex-snapshot

NETosis is an important component of chronic inflammation in patients with heart failure

inferred← citeshttps://doi.org/10.1111/aji.12617openalex-snapshot

Neutrophil extracellular traps in acute chorioamnionitis: A mechanism of host defense

inferred← citeshttps://doi.org/10.1111/aji.12723openalex-snapshot

Amniotic fluid neutrophils can phagocytize bacteria: A mechanism for microbial killing in the amniotic cavity

inferred← citeshttps://doi.org/10.1111/all.12111openalex-snapshot

Extracellular DNA traps in allergic, infectious, and autoimmune diseases

inferred← citeshttps://doi.org/10.1111/bjd.15839openalex-snapshot

Dimethyl fumarate modulates neutrophil extracellular trap formation in a glutathione‐ and superoxide‐dependent manner

inferred← citeshttps://doi.org/10.1111/bjd.19800openalex-snapshot

Modular gene analysis reveals distinct molecular signatures for subsets of patients with cutaneous lupus erythematosus*

inferred← citeshttps://doi.org/10.1111/bjh.12608openalex-snapshot

Traps and hyper inflammation – new ways that neutrophils promote or hinder survival

inferred← citeshttps://doi.org/10.1111/brv.12522openalex-snapshot

Root extracellular traps versus neutrophil extracellular traps in host defence, a case of functional convergence?

inferred← citeshttps://doi.org/10.1111/cmi.12320openalex-snapshot

The complex roles of NADPH oxidases in fungal infection

inferred← citeshttps://doi.org/10.1111/cmi.12649openalex-snapshot

Neutrophil extracellular trap formation in theStreptococcus suis-infected cerebrospinal fluid compartment

inferred← citeshttps://doi.org/10.1111/exd.12599openalex-snapshot

The NET , the trap and the pathogen: neutrophil extracellular traps in cutaneous immunity

inferred← citeshttps://doi.org/10.1111/exd.13125openalex-snapshot

Interindividual variation of NET osis in healthy donors: introduction and application of a refined method for extracellular trap quantification

inferred← citeshttps://doi.org/10.1111/febs.16036openalex-snapshot

Recent progress in the mechanistic understanding of NET formation in neutrophils

inferred← citeshttps://doi.org/10.1111/j.1365-2796.2011.02432.xopenalex-snapshot

High-mobility group box 1 represents a potential marker of disease activity and novel therapeutic target in systemic lupus erythematosus

inferred← citeshttps://doi.org/10.1111/j.1600-0765.2008.01175.xopenalex-snapshot

Extracellular neutrophil traps in periodontitis

inferred← citeshttps://doi.org/10.1111/jch.14942openalex-snapshot

Role of Neutrophil Extracellular Traps in Hypertension and Their Impact on Target Organs

inferred← citeshttps://doi.org/10.1111/jcmm.12550openalex-snapshot

Belinostat, a potent HDAC i, exerts antileukaemic effect in human acute promyelocytic leukaemia cells via chromatin remodelling

inferred← citeshttps://doi.org/10.1111/jcmm.71306openalex-snapshot

Increased NETosis in Patients With Heart Failure Is Associated With Macrophage Activation Towards a Proinflammatory Phenotype

inferred← citeshttps://doi.org/10.1111/vec.12592openalex-snapshot

Measurement of plasma cell‐free DNA concentrations in dogs with sepsis, trauma, and neoplasia

inferred← citeshttps://doi.org/10.1126/stke.121pe25openalex-snapshot

ETosis: A Novel Cell Death Pathway

inferred← citeshttps://doi.org/10.1128/9781683670131.ch9openalex-snapshot

Group AStreptococcus-Mediated Host Cell Signaling

inferred← citeshttps://doi.org/10.1128/iai.02487-14openalex-snapshot

Cyclic AMP-Mediated Suppression of Neutrophil Extracellular Trap Formation and Apoptosis by the Bordetella pertussis Adenylate Cyclase Toxin

inferred← citeshttps://doi.org/10.1128/jb.00006-24openalex-snapshot

Multitasking functions of bacterial extracellular DNA in biofilms

inferred← citeshttps://doi.org/10.1128/microbiolspec.gpp3-0021-2018openalex-snapshot

Group AStreptococcus-Mediated Host Cell Signaling

inferred← citeshttps://doi.org/10.1128/mmbr.00052-22openalex-snapshot

Interplay between group A Streptococcus and host innate immune responses

inferred← citeshttps://doi.org/10.1134/s0006297912070073openalex-snapshot

The phenoptosis problem: What is causing the death of an organism? Lessons from acute kidney injury

inferred← citeshttps://doi.org/10.1134/s0006297914120025openalex-snapshot

Neutrophil Extracellular Traps: Mechanisms of formation and role in health and disease

inferred← citeshttps://doi.org/10.1134/s0006297920100065openalex-snapshot

NETosis: Molecular Mechanisms, Role in Physiology and Pathology

inferred← citeshttps://doi.org/10.1134/s0362119726700362openalex-snapshot

Migration and Functional Activity of Tissue Leukocytes in Practically Healthy Residents of the Northern Territories of the European Territory of the Russian Federation

inferred← citeshttps://doi.org/10.1136/rmdopen-2023-003104openalex-snapshot

Neutrophil extracellular traps (NET): not only antimicrobial but also modulators of innate and adaptive immunities in inflammatory autoimmune diseases

inferred← citeshttps://doi.org/10.1136/vetreco-2019-000357openalex-snapshot

Effect of sample type on plasma concentrations of cell‐free DNA and nucleosomes in dogs

inferred← citeshttps://doi.org/10.1155/2012/849136openalex-snapshot

The Impact of Various Reactive Oxygen Species on the Formation of Neutrophil Extracellular Traps

inferred← citeshttps://doi.org/10.1155/2013/651497openalex-snapshot

NETosis

inferred← citeshttps://doi.org/10.1155/2016/4604713openalex-snapshot

How Neutrophil Extracellular Traps Become Visible

inferred← citeshttps://doi.org/10.1155/2017/4915062openalex-snapshot

Neutrophil Extracellular Trap Production in Patients with Colorectal Cancer In Vitro

inferred← citeshttps://doi.org/10.1155/2019/3560180openalex-snapshot

Nanomaterial Exposure Induced Neutrophil Extracellular Traps: A New Target in Inflammation and Innate Immunity

inferred← citeshttps://doi.org/10.1155/2020/4192745openalex-snapshot

In Vivo Imaging of Neutrophil Extracellular Traps (NETs): Visualization Methods and Outcomes

inferred← citeshttps://doi.org/10.1155/2022/3235524openalex-snapshot

Role of NETosis in Central Nervous System Injury

inferred← citeshttps://doi.org/10.1159/000205281openalex-snapshot

Mouse Neutrophil Extracellular Traps in Microbial Infections

inferred← citeshttps://doi.org/10.1159/000489829openalex-snapshot

Neutrophil Extracellular Traps in the Second Decade

inferred← citeshttps://doi.org/10.11606/d.41.2019.tde-18022019-165436openalex-snapshot

Evolução das vias de controle do desenvolvimento tecidual em holometábolos

inferred← citeshttps://doi.org/10.11606/d.60.2016.tde-02052016-145116openalex-snapshot

Ação imunomoduladora do esteroide dehidroepiandrosterona (DHEA) na resposta efetora de neutrófilos infectados in vitro por Salmonella enterica serovar Typhimurium

inferred← citeshttps://doi.org/10.11606/t.42.2019.tde-02102019-152220openalex-snapshot

Importância do complexo 2 da via mTOR (mTORC2) nas funções efetoras e no metabolismo dos neutrófilos em modelo experimental de SEPSE

inferred← citeshttps://doi.org/10.11606/t.42.2020.tde-16122019-161916openalex-snapshot

O papel dos neutrófilos e dos receptores TLR-2 e TLR-4 na cromoblastomicose experimental em infecção por >i /i<

inferred← citeshttps://doi.org/10.1161/circresaha.119.314581openalex-snapshot

Extracellular DNA NET-Works With Dire Consequences for Health

inferred← citeshttps://doi.org/10.1164/rccm.201708-1590ocopenalex-snapshot

E-Cigarette Use Causes a Unique Innate Immune Response in the Lung, Involving Increased Neutrophilic Activation and Altered Mucin Secretion

inferred← citeshttps://doi.org/10.1177/03009858211005537openalex-snapshot

Mechanisms of Regulated Cell Death: Current Perspectives

inferred← citeshttps://doi.org/10.1177/10760296261462870openalex-snapshot

Citrullinated Histone 3 as a Marker of NETosis at Opposite Ends of Hemostasis: Evidence From Thrombosis-Prone MPN and Bleeding-Prone Hemophilia

inferred← citeshttps://doi.org/10.1177/20480040251399336openalex-snapshot

Cholesterol microcrystals and neutrophil extracellular traps detection during open aortic surgery

inferred← citeshttps://doi.org/10.1182/blood-2007-07-104018openalex-snapshot

Phagocytosis-independent antimicrobial activity of mast cells by means of extracellular trap formation

inferred← citeshttps://doi.org/10.1182/blood-2013-04-457671openalex-snapshot

NETosis: how vital is it?

inferred← citeshttps://doi.org/10.1182/blood-2018-11-844530openalex-snapshot

Neutrophils and NETs in modulating acute and chronic inflammation

inferred← citeshttps://doi.org/10.1186/s12950-023-00334-1openalex-snapshot

Transient receptor potential melastatin 2 regulates neutrophil extracellular traps formation and delays resolution of neutrophil-driven sterile inflammation

inferred← citeshttps://doi.org/10.1186/s12950-023-00344-zopenalex-snapshot

Neutrophil extracellular traps in acute coronary syndrome

inferred← citeshttps://doi.org/10.1186/s12950-026-00490-0openalex-snapshot

Simplified flow cytometric quantification of human neutrophil extracellular traps (NETs)

inferred← citeshttps://doi.org/10.1186/s12959-023-00512-4openalex-snapshot

The effect of neutrophil extracellular traps in venous thrombosis

inferred← citeshttps://doi.org/10.1186/s12964-024-01563-4openalex-snapshot

A promising frontier: targeting NETs for stroke treatment breakthroughs

inferred← citeshttps://doi.org/10.1186/s13045-026-01789-4openalex-snapshot

Neutrophil extracellular traps in the tumor microenvironment, metastasis, therapy, and beyond: advances, challenges, and perspectives

inferred← citeshttps://doi.org/10.1186/s13578-021-00708-zopenalex-snapshot

The regulatory mechanism of neutrophil extracellular traps in cancer biological behavior

inferred← citeshttps://doi.org/10.1186/s42826-025-00247-5openalex-snapshot

Comparative transcriptome analysis of PBMCs in cats diagnosed with and recovered from FIPV

inferred← citeshttps://doi.org/10.1189/jlb.1108715openalex-snapshot

Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss–of–function mutation in the gene for cytochrome b(–245), alpha polypeptide (Cyba)

inferred← citeshttps://doi.org/10.1189/jlb.1211601openalex-snapshot

Requirements for NADPH oxidase and myeloperoxidase in neutrophil extracellular trap formation differ depending on the stimulus

inferred← citeshttps://doi.org/10.1189/jlb.5bt0615-247ropenalex-snapshot

At the Bench: Neutrophil extracellular traps (NETs) highlight novel aspects of innate immune system involvement in autoimmune diseases

inferred← citeshttps://doi.org/10.1194/jlr.m084731openalex-snapshot

2-Chlorofatty acids: lipid mediators of neutrophil extracellular trap formation

inferred← citeshttps://doi.org/10.1242/jcs.241075openalex-snapshot

The power from within – understanding the driving forces of neutrophil extracellular trap formation

inferred← citeshttps://doi.org/10.12703/r/9-25openalex-snapshot

Phagocytosis and neutrophil extracellular traps

inferred← citeshttps://doi.org/10.1371/journal.pone.0092129openalex-snapshot

The Anti-Oxidative Role of Micro-Vesicles Derived from Human Wharton-Jelly Mesenchymal Stromal Cells through NOX2/gp91(phox) Suppression in Alleviating Renal Ischemia-Reperfusion Injury in Rats

inferred← citeshttps://doi.org/10.1371/journal.pone.0279944openalex-snapshot

Extracellular histone release by renal cells after warm and cold ischemic kidney injury: Studies in an ex-vivo porcine kidney perfusion model

inferred← citeshttps://doi.org/10.1371/journal.ppat.1000639openalex-snapshot

Neutrophil Extracellular Traps Contain Calprotectin, a Cytosolic Protein Complex Involved in Host Defense against Candida albicans

inferred← citeshttps://doi.org/10.14336/ad.2024.0129openalex-snapshot

Immunological Landscape of Retinal Ischemia-Reperfusion Injury: Insights into Resident and Peripheral Immune Cell Responses

inferred← citeshttps://doi.org/10.1515/cclm-2021-0172openalex-snapshot

Critical role of pre-analytical aspects for the measurement of circulating calprotectin in serum or plasma as a biomarker for neutrophil-related inflammation

inferred← citeshttps://doi.org/10.1517/14728222.2014.953929openalex-snapshot

Antithrombotic therapy: new areas to understand efficacy and bleeding

inferred← citeshttps://doi.org/10.2139/ssrn.4985171openalex-snapshot

Quercetin Alleviates Severe Pneumonia Induced by H1n1 and Mrsa Co-Infection Through the Inhibition of Neutrophil Extracellular Trap Formation

inferred← citeshttps://doi.org/10.2147/copd.s115969openalex-snapshot

Evidence of eosinophil extracellular trap cell death in COPD: does it represent the trigger that switches on the disease?

inferred← citeshttps://doi.org/10.2147/ijgm.s583609openalex-snapshot

Neutrophil Extracellular Traps in Dry Eye: A Comprehensive Review of Pathogenic Mechanisms and Implications for Targeted Therapy

inferred← citeshttps://doi.org/10.2147/jir.s362066openalex-snapshot

Bacteriocin BacSp222 and Its Succinylated Forms Exhibit Proinflammatory Activities Toward Innate Immune Cells

inferred← citeshttps://doi.org/10.21608/ejhm.2023.320234openalex-snapshot

The Potential Role of Neutrophils in Enhancement of Thrombotic Risk in Patients with Primary Antiphospholipid Syndrome

inferred← citeshttps://doi.org/10.23868/gc352562openalex-snapshot

NEUTROPHIL EXTRACELLULAR TRAPS: STRUCTURE AND BIOLOGICAL ROLE

inferred← citeshttps://doi.org/10.23880/ijbp-16000222openalex-snapshot

Revisiting Pyronin Y, A Classical Photostable Xanthene Dye useful for Cost Effective Multimodal Fluorescence Microscopy

inferred← citeshttps://doi.org/10.23934/2223-9022-2022-11-3-484-492openalex-snapshot

Immunopathogenesis of Acute Pancreatitis

inferred← citeshttps://doi.org/10.26502/ami.9365003openalex-snapshot

Neutrophil Extracellular Trap (NET): The Interplay Between Infection, Inflammation and Thrombosis

inferred← citeshttps://doi.org/10.26599/oshm.2026.9610051openalex-snapshot

Multilayered molecular architecture orchestrating programmed cell death in mucosal barriers tissues

inferred← citeshttps://doi.org/10.29328/journal.jsctt.1001020openalex-snapshot

Neutrophils, NETs, NETosis and their paradoxical roles in COVID-19

inferred← citeshttps://doi.org/10.3103/s0096392520030104openalex-snapshot

NADPH Oxidase Modulates Ca2+-Dependent Formation of Neutrophil Extracellular Traps

inferred← citeshttps://doi.org/10.3103/s0096392520040112openalex-snapshot

Neutrophil Extracellular Traps: New Aspects

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